FDA UDI In Commercial Distribution 🇺🇸 United States

REDUX

DI: 03596010381682 · Model: 014770 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REDUX
Primary DI
03596010381682
Version / Model
014770
Catalog Number
014770
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
64937f9e-e165-4182-8583-d8ff7fe069b6

Device Description

REDUX 3.4 MM DRIVER

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 03596010381682

Customer Contacts